Pharmaceutical Manufacturing seeks a Regulatory Affairs Associate. Resp. include preparing and maintaining Standard Operating Procedures, Out of Specs Report, annual reports and investigations, coordinate regulatory documentation activities, assist in preparing regulatory documents, support the development and implementation of regulatory strategies, ensure regulatory compliance. Applicant must possess a Master’s Degree in Pharmaceutical Technology/Regulatory Affairs for Drugs, Biologics & Medical Devices/Regulatory Affairs with 3 months of experience. 40 hrs/wk M-F. Mail Resumes ref. to job # SP001 Sunrise Pharmaceuticals Inc. 665 East Lincoln Ave., Rahway, NJ 07065.